Journal of Precision Biosciences
Biopharmaceuticals and medical sciences | Online ISSN 3064-9226
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RESEARCH ARTICLE   (Open Access)
Contents Vol 1 (1)

Integrative Analysis of WES and Proteomics in Progressive CNS Inflammation Autoimmune Disease: Insights and Therapeutic Strategies

Md Shamsuddin Sultan Khan 1*, Anton Yuryev 2, John Catanzaro 3

+ Author Affiliations

Journal of Precision Biosciences 1 (1) 1-6 https://doi.org/10.25163/biosciences.112089DB112921119

Submitted: 11 October 2019 Revised: 29 October 2019  Published: 02 November 2019 

Abstract

Background: Progressive central nervous system (CNS) inflammation autoimmune diseases present significant diagnostic and therapeutic challenges due to their complex pathology and variability. Advanced immuno-molecular techniques such as Whole Exome Sequencing (WES) and proteomics offer promising insights into these disorders. The PBIMA (Progressive CNS Inflammation Autoimmune Disease Sample Report) aims to elucidate the genetic and proteomic underpinnings of such diseases, with a focus on understanding the mechanisms and identifying potential therapeutic targets. Methods: This report integrates WES and proteomic data to explore the molecular basis of progressive CNS inflammation autoimmune diseases. Genetic profiling included HLA compatibility and affinity typing using advanced tools such as Neo7Logix's Biological/PPI Pathway Studio and HLA-NetMHCII2. Key genes and proteins associated with disease mechanisms were identified, including COL1A1, COL5A1, IFIH1, and IL6R. The study also investigated the role of citrullinated MBP sequences in autoantigenic inflammation and explored innovative treatment approaches such as integrative intravenous (IV) therapies, injection therapies, and advanced cell therapy. Results: The HLA typing revealed specific alleles linked to autoimmune susceptibility, and the genetic analysis identified significant variants in genes related to connective tissue disorders, immune responses, and inflammatory pathways. Proteomic data highlighted the involvement of proteins like MBP and cytokine receptors in disease progression. The therapeutic strategies, including integrative IV design and targeted immuno-molecular treatments, were tailored to the patient's genetic and immunological profile, demonstrating potential for managing autoimmune inflammation effectively. Conclusion: The PBIMASM report demonstrates the utility of combining WES and proteomic data to advance the understanding of progressive CNS inflammation autoimmune diseases. The integration of genetic, immunological, and therapeutic insights facilitates the development of personalized treatment approaches, offering a promising framework for improving diagnostic accuracy and therapeutic outcomes in managing these complex disorders. Future research should further evaluate the effectiveness of these combined strategies and explore their applicability to broader patient populations.

Keywords: Progressive CNS Inflammation, Autoimmune Disease, Whole Exome Sequencing, Proteomics, Immunological Profiling

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